Prospective Study
Copyright ©The Author(s) 2019.
World J Clin Cases. Sep 26, 2019; 7(18): 2734-2745
Published online Sep 26, 2019. doi: 10.12998/wjcc.v7.i18.2734
Figure 1
Figure 1 Box plots of observed species, Chao1 index, and Shannon and Simpson indices of microbiota for healthy subjects and systemic-onset juvenile idiopathic arthritis patients with different disease activities. Medians and interquartile ranges are shown. The significance of differences was calculated using the Kruskal-Wallis test with Bonferroni correction. aP < 0.001, A-SoJIA vs HS in observed species; bP < 0.01, Ina-SoJIA vs HS in observed species; cP < 0.001, A-SoJIA vs HS in Chao1; dP < 0.01, Ina-SoJIA vs HS in Chao1. SoJIA: Systemic-onset juvenile idiopathic arthritis; A-SoJIA: Active-SoJIA; Ina-SoJIA: Inactive-SoJIA; HS: Healthy subjects.
Figure 2
Figure 2 Principal coordinate analysis based on the overall structure of the stool microbiota in all samples. A: Principal coordinate analysis (PCoA) of Bray-Curtis dissimilarities; B: PCoA of unweighted UniFrac dissimilarities. Each data point represents an individual sample. Red: Active-SoJIA; Blue: Inactive-SoJIA; Green: Healthy subject samples.
Figure 3
Figure 3 Relative abundances of fecal bacterial components in systemic-onset juvenile idiopathic arthritis and healthy subjects groups. A: Box plots of Firmicutes; B: Box plots of Bacteroidetes; C: Box plots of Firmicutes/Bacteroidetes ratio; D-I: Box plots of statistically significantly different bacteria at levels below phylum. Significance was calculated by the Kruskal-Wallis test with Bonferroni correction.
Figure 4
Figure 4 Associations between gut microbiota profile and clinicopathological features in systemic-onset juvenile idiopathic arthritis patients at the (A) phylum, (B) family, and (C) genus levels. DD: Disease duration; CRP: C-reactive protein; ESR: Erythrocyte sedimentation rate; JADAS: Juvenile arthritis disease activity score.